2-methyl-Δ⁸-tetrahydrocannabinol | 36403-83-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 2-methyl-Δ⁸-tetrahydrocannabinol
• 英文别名: Δ-9-tetrahydrocannabinol；Δ-9-THC；4'-Methyl-Δ¹-THC；(6aR,10aR)-2,6,6,9-tetramethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol
• CAS: 36403-83-5
• 化学式: C₂₂H₃₂O₂
• 分子量: 328.495
• InChiKey: CNCURDLLOPZUIO-QZTJIDSGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.3
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  cannabidiolic acid methyl ester 在 lithium aluminium tetrahydride 、 silica gel 、 对甲苯磺酸 作用下， 生成 2-methyl-Δ⁸-tetrahydrocannabinol
  参考文献：
  名称：

  2-Methyl- and 4-Methyl-D8-tetrahydrocaniiabinol: Correlation of Spatial Distinction with Cannabinoid Receptor Binding

  摘要：

  A high level of binding to the brain cannabinoid receptor was found for 2-methyl-Delta(8)-tetrahydrocannabinol (THC) while no binding was observed for 4-methyl-Delta(8)-THC. Four energy minima were found by molecular mechanics for ethyl side-chain models of Delta(8)-THC [syn- and antiperiplanar and (+/-)-orthogonal values for torsion angle C(4)-C(3)-C(alpha)-C(beta)]. The active Delta(8)-THC and 2-methyl-Delta(8)-THC molecules share a common structural feature [a relatively low energy synperiplanar value C(4)-C(3)-C(alpha)-C(beta) torsion angle conformation for the n-pentyl side chain] that is not exhibited by the inactive 4-methyl-Delta(8)-THC analogue. This spatial distinction may represent the basis for the difference in biological activity between the tn two isomers examined.

  DOI：

  10.3987/com-94-s(b)86

文献信息

• [EN] PROCESS FOR THE SYNTHESIS AND PURIFICATION OF CANNABINOIC ACIDS AND ACYLATED DERIVATIVES THEREOF<br/>[FR] PROCÉDÉ DE SYNTHÈSE ET DE PURIFICATION D'ACIDES CANNABINOÏDES ET DE DÉRIVÉS ACYLÉS DE CEUX-CI
  申请人：[en]TRESCO LABS GMBH

  公开号：WO2023099549A1

  公开（公告）日：2023-06-08

  The invention relates to a novel process for the synthesis and/or purification of tetrahydro-cannabinolic acid (THCA) alkanoates and/or cannabidiolic acid (CBDA) di- alkanoates. The invention also provides novel derivatives of CBDA di-alkanoates and THCA alkanoates according to Formula (I).
• 2-Methyl- and 4-Methyl-D8-tetrahydrocaniiabinol: Correlation of Spatial Distinction with Cannabinoid Receptor Binding
  作者：Robert Glaser、Itay Adin、Raphael Machoulam、Lumir Hanus

  DOI：10.3987/com-94-s(b)86

  日期：——

  A high level of binding to the brain cannabinoid receptor was found for 2-methyl-Delta(8)-tetrahydrocannabinol (THC) while no binding was observed for 4-methyl-Delta(8)-THC. Four energy minima were found by molecular mechanics for ethyl side-chain models of Delta(8)-THC [syn- and antiperiplanar and (+/-)-orthogonal values for torsion angle C(4)-C(3)-C(alpha)-C(beta)]. The active Delta(8)-THC and 2-methyl-Delta(8)-THC molecules share a common structural feature [a relatively low energy synperiplanar value C(4)-C(3)-C(alpha)-C(beta) torsion angle conformation for the n-pentyl side chain] that is not exhibited by the inactive 4-methyl-Delta(8)-THC analogue. This spatial distinction may represent the basis for the difference in biological activity between the tn two isomers examined.